Viewing Study NCT06573151



Ignite Creation Date: 2024-10-26 @ 3:38 PM
Last Modification Date: 2024-10-26 @ 3:38 PM
Study NCT ID: NCT06573151
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-08-16

Brief Title: Selinexor Anti-PD-1 Antibody and P-GemOx Regimen in RR NKTCL
Sponsor: None
Organization: None

Study Overview

Official Title: The Efficacy and Safety of Selinexor Anti-PD-1 Antibody and P-GemOx Regimen in the Treatment of Relapsed or Refractory Natural Killer T-cell Lymphoma
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: A multicenter prospective trial to evaluate the efficacy and safety of Selinexor anti-PD-1 antibody and P-GemOx in the treatment of relapsed or refractory Natural Killer T-cell lymphoma
Detailed Description: This study aims to evaluate the efficacy and safety of Selinexor anti-PD-1 antibody plus P-GemOx in relapsed or refractory NKTCL and find the optimal treatment regimen for patients with relapsed refractory NKTCL

Patients receive 3 cycles of Selinexor anti-PD-1 antibody plus P-GemOx and then PET evaluation

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None